2-(Trifluoromethoxy)benzene-1-sulfonyl chloride → HCID 49800501, compound
Reaction equation
C(O[C:4]([C:6]1([CH2:12][CH2:13]OC)[CH2:11][CH2:10][NH:9][CH2:8][CH2:7]1)=[O:5])C.[F:16][C:17]([F:30])([F:29])[O:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=1[S:25](Cl)(=[O:27])=[O:26].[CH:31]1([C:34]2[CH:40]=[CH:39][C:37]([NH2:38])=[CH:36][CH:35]=2)[CH2:33][CH2:32]1>>[CH:31]1([C:34]2[CH:40]=[CH:39][C:37]([N:38]3[CH2:13][CH2:12][C:6]4([CH2:7][CH2:8][N:9]([S:25]([C:20]5[CH:21]=[CH:22][CH:23]=[CH:24][C:19]=5[O:18][C:17]([F:30])([F:29])[F:16])(=[O:27])=[O:26])[CH2:10][CH2:11]4)[C:4]3=[O:5])=[CH:36][CH:35]=2)[CH2:33][CH2:32]1Participants
4
Procedure
Off-white solid. MS (ESI): 495.15 (MH+). This example was prepared in analogy to example 1 step C) to D) from 4-(2-methoxy-ethyl)-piperidine-4-carboxylic acid ethyl ester (example 1 step B)), 2-trifluoromethoxy-benzenesulfonyl chloride and 4-(cyclopropyl)-aniline.
Sources & evidence
- ORD record
- ord-b4adfd06757d40e8b1aa95c7afa79710
- Source dataset
- uspto-grants-2012_12
- Patent number
- US08329904B2
Reaction notes
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